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Phenotypic Abnormality (PA): Recurrent infections

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the immune system [HP:0002715] <3>(37|52) (39|28|15)
+ + 2:   Abnormality of immune system physiology [HP:0010978] <14>(29|40) (31|23|11)
+ 1:   Unusual infection [HP:0032101] <11>(15|20) (17|7|0)
0:   Recurrent infections [HP:0002719] <15>(6|13) (8|5|0)
- 1:   Recurrent respiratory infections [HP:0002205] <8>(2|6) (3|3|0)
- 1:   Recurrent bacterial infections [HP:0002718] <6>(3|3) (3|1|0)
- 1:   Recurrent fungal infections [HP:0002841] <6>(0|0) (0|0|0)
- 1:   Recurrent viral infections [HP:0004429] <6>(0|0) (0|1|0)
- 1:   Recurrent infection of the gastrointestinal tract [HP:0004798] <3>(0|0) (0|0|0)
- 1:   Recurrent urinary tract infections [HP:0000010] <2>(0|1) (0|0|0)
- 1:   Recurrent abscess formation [HP:0002722] <1>(0|0) (0|0|0)
- 1:   Recurrent protozoan infections [HP:0005386] <1>(0|0) (0|0|0)
- 1:   Failure to thrive secondary to recurrent infections [HP:0008866](0|0) (0|0|0)
- 1:   Recurrent ear infections [HP:0410018](0|0) (0|0|0)
- 1:   Recurrent infections in infancy and early childhood [HP:0005437](0|0) (0|0|0)
- 1:   Recurrent infections of the middle ear [HP:0040268](0|0) (0|0|0)
- 1:   Recurrent opportunistic infections [HP:0005390](0|0) (0|0|0)
- 1:   Recurrent otitis media [HP:0000403](0|1) (0|0|0)
- 1:   Recurrent parasitic infections [HP:0030885](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
(Trans)glycosidases0.0007986Direct
Complement control module/SCR domain0.005594Inherited
ABC transporter transmembrane region0.3415Inherited
LDL receptor-like module0.4337Inherited
TSP-1 type 1 repeat0.7867Inherited
TNF receptor-like0.9598Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
beta-glycanases0Direct
C1 set domains (antibody constant domain-like)0.0004226Direct
TNF-like0.0008272Direct
Complement control module/SCR domain0.003214Inherited
Notch domain0.003833Inherited
Rel/Dorsal transcription factors, DNA-binding domain0.003833Inherited
Arylsulfatase0.008637Inherited
RecA protein-like (ATPase-domain)0.1229Inherited
ABC transporter transmembrane region0.1884Inherited
I set domains0.291Inherited
LDL receptor-like module0.3831Inherited
ABC transporter ATPase domain-like0.5628Inherited
TSP-1 type 1 repeat0.7536Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
(Trans)glycosidases0.0004278Direct
TNF-like0.0008849Direct
Complement control module/SCR domain0.003486Inherited
Notch domain0.003955Inherited
ABC transporter transmembrane region0.3013Inherited
LDL receptor-like module0.3907Inherited
TSP-1 type 1 repeat0.752Inherited
TNF receptor-like0.9351Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.0008684Direct
    49417,81296
  • 49417 - p53-like transcription factors
  • 81296 - E set domains
  • 0.003955Inherited
    55550,56112
  • 55550 - SH2 domain
  • 56112 - Protein kinase-like (PK-like)
  • 0.004864Inherited
    53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.01291Inherited
    90123,52540
  • 90123 - ABC transporter transmembrane region
  • 52540 - P-loop containing nucleoside triphosphate hydrolases
  • 0.3013Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
    (show help)